Tail Snip Homogenization Using the Bullet Blender

Materials

Bullet Blender^® for 1.5 mL tubes
Homogenization Buffer
FoamBlocker (Optional)
Lysis Kit or Lysis Beads
- GREEN or NAVY Lysis Kit (from PrecisionPak™ or purchased separately)
- 1.4 mm blend + 3.2 mm Stainless Steel Beads in Eppendorf, GATOR, or RINO tubes
Sample — up to 300 mg

Table 1. Proper sample, bead and buffer volume ratios for 1.5 mL tubes.

Lysis Kit and Bead Choices	Sample Volume	Bead Volume	Buffer Volume
GREEN	Up to 100 mg	Pre-filled	200 - 300 µL
NAVY	100 - 300 mg	Pre-filled	300 - 600 µL
1.4 mm blend + 3.2 mm Stainless Steel Beads	Up to 300 mg	100 - 200 µL	200 - 600 µL

Procedure

Use the pre-filled bead lysis kit tubes OR prepare a tube with the recommended volume of bead choices from the table above.
Add the appropriate volume of buffer according to the table above.
Prepare the sample by cutting it into small thin pieces and then transfer it into the buffer-filled tubes.
(Optional) To avoid excess foaming, add FoamBlocker up to 1-2% of the total volume of the homogenization buffer.
Close the tubes tightly and place into the Bullet Blender sample chamber. If using the Gold or Gold⁺ models, pre-cool the chamber before adding sample tubes.
Set the controls to speed 12, time 3 minutes then press Start.

Note: Using single-size beads instead of pre-filled lysis kits may require additional time.
After the run, remove the tubes from the instrument and visually inspect the samples. If homogenization is incomplete, homogenize for an additional 30 seconds, or repeat the homogenization step with a higher speed.
Using a pipette, transfer the homogenized samples into new tubes.
Proceed with downstream application.

Notes

This protocol does not specify a particular buffer – choose a buffer that is most appropriate for the downstream application or use the lysis buffer provided in a PrecisionPak™, a simplified workflow solution which also includes a bead lysis kit, supplemental reagents for high quality nucleic acids isolations, and an optimized protocol for specific samples.

This protocol was developed using mouse tissue. Homogenization times, speeds, or beads may need to be optimized for other species, especially larger animals.